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WO2018150379A3 - Synthesis of pheromones and related materials via olefin metathesis - Google Patents

Synthesis of pheromones and related materials via olefin metathesis Download PDF

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Publication number
WO2018150379A3
WO2018150379A3 PCT/IB2018/050980 IB2018050980W WO2018150379A3 WO 2018150379 A3 WO2018150379 A3 WO 2018150379A3 IB 2018050980 W IB2018050980 W IB 2018050980W WO 2018150379 A3 WO2018150379 A3 WO 2018150379A3
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WO
WIPO (PCT)
Prior art keywords
pheromones
synthesis
olefin metathesis
related materials
materials via
Prior art date
Application number
PCT/IB2018/050980
Other languages
French (fr)
Other versions
WO2018150379A2 (en
Inventor
Keith M. Wampler
Vu Bui
David Rozzell
Pedro COELHO
Arthur FLORUTI
Levente Ondi
Hasan MEHDI
Gabor EROS
Original Assignee
Provivi, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Provivi, Inc. filed Critical Provivi, Inc.
Priority to EP18753853.3A priority Critical patent/EP3583088B1/en
Priority to JP2019544718A priority patent/JP7153937B2/en
Priority to CN201880023250.3A priority patent/CN110603240B/en
Publication of WO2018150379A2 publication Critical patent/WO2018150379A2/en
Publication of WO2018150379A3 publication Critical patent/WO2018150379A3/en
Priority to US16/543,384 priority patent/US11155505B2/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/32Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
    • C07C1/321Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a non-metal atom
    • C07C1/322Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a non-metal atom the hetero-atom being a sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/09Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/095Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of organic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/09Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/10Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
    • C07C29/103Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/32Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/58Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of halogen, e.g. by hydrogenolysis, splitting-off
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/08Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/28Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/293Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/64Molybdenum
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/66Tungsten
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Methods for preparation of olefins, including 8- and 11-unsaturated monoenes and polyenes, via transition metathesis-based synthetic routes are described. Metathesis reactions in the methods are catalyzed by transition metal catalysts including tungsten-, molybdenum-, and ruthenium-based catalysts. The olefins include insect pheromones useful in a number of agricultural applications.
PCT/IB2018/050980 2017-02-17 2018-02-17 Synthesis of pheromones and related materials via olefin metathesis WO2018150379A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP18753853.3A EP3583088B1 (en) 2017-02-17 2018-02-17 Synthesis of pheromones and related materials via olefin metathesis
JP2019544718A JP7153937B2 (en) 2017-02-17 2018-02-17 Synthesis of pheromones and related materials by olefin metathesis
CN201880023250.3A CN110603240B (en) 2017-02-17 2018-02-17 Synthesis of pheromones and related substances by olefin metathesis
US16/543,384 US11155505B2 (en) 2017-02-17 2019-08-16 Synthesis of pheromones and related materials via olefin metathesis

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201762460661P 2017-02-17 2017-02-17
US201762460667P 2017-02-17 2017-02-17
US62/460,667 2017-02-17
US62/460,661 2017-02-17
US201762511903P 2017-05-26 2017-05-26
US62/511,903 2017-05-26

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/543,384 Continuation US11155505B2 (en) 2017-02-17 2019-08-16 Synthesis of pheromones and related materials via olefin metathesis

Publications (2)

Publication Number Publication Date
WO2018150379A2 WO2018150379A2 (en) 2018-08-23
WO2018150379A3 true WO2018150379A3 (en) 2018-11-08

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PCT/IB2018/050980 WO2018150379A2 (en) 2017-02-17 2018-02-17 Synthesis of pheromones and related materials via olefin metathesis

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US (1) US11155505B2 (en)
EP (1) EP3583088B1 (en)
JP (1) JP7153937B2 (en)
CN (1) CN110603240B (en)
WO (1) WO2018150379A2 (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9919299B2 (en) 2013-03-14 2018-03-20 Ximo Ag Metathesis catalysts and reactions using the catalysts
US10427146B2 (en) 2013-10-01 2019-10-01 Ximo Ag Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis
CN110603240B (en) 2017-02-17 2022-11-15 普罗维维公司 Synthesis of pheromones and related substances by olefin metathesis
US12049443B2 (en) 2018-12-10 2024-07-30 Provivi, Inc. Synthesis of conjugated diene pheromones and related compounds
WO2020239859A1 (en) * 2019-05-27 2020-12-03 Verbio Vereinigte Bioenergie Ag Tungsten imido alkylidene o-bitet and o-binol complexes and use thereof in olefin metathesis reactions
EP3999230A1 (en) * 2019-07-17 2022-05-25 California Institute of Technology New syntheses of z-selective olefin metathesis catalysts
MX2022015178A (en) * 2020-06-01 2023-03-01 Provivi Inc Synthesis of pheromone derivatives via z-selective olefin metathesis.
CN111961856B (en) * 2020-07-06 2022-01-07 廖乐 Device for separating vanadium and rare earth elements from waste FCC catalyst
JP7377783B2 (en) * 2020-10-02 2023-11-10 信越化学工業株式会社 Haloalkenyl alkoxymethyl ether compound and method for producing a terminally conjugated alkadien-1-yl acetate compound and a terminally conjugated alkadien-1-ol compound using the same
JP7349969B2 (en) 2020-10-02 2023-09-25 信越化学工業株式会社 6-hydroxy-3-hexenyl alkoxymethyl ether compound and method for producing 3,13-octadecadien-1-ol compound using the same
CN112782309B (en) * 2020-12-29 2022-10-28 常州大学 Method for stabilizing long-chain unsaturated olefine aldehyde
FR3123356B1 (en) * 2021-05-28 2023-04-28 Melchior Material & Life Science France New continuous pheromone manufacturing process
CN113480428B (en) * 2021-06-30 2022-02-15 中捷四方生物科技股份有限公司 Method for preparing trans-7, cis-9-dodecadieneacetic ester
CN113398993B (en) * 2021-07-20 2022-07-12 厦门大学 A kind of catalyst and its preparation method and application
CN115124405B (en) * 2022-09-01 2022-11-11 山东新和成药业有限公司 Method for preparing leaf alcohol by isomerizing 4-hexene-1-alcohol and ruthenium-based catalyst used in method
WO2024081627A1 (en) * 2022-10-10 2024-04-18 Provivi, Inc. Storage stable pheromone compositions and systems
JP2024063756A (en) * 2022-10-26 2024-05-13 信越化学工業株式会社 Organic halogen compounds having conjugated double bonds, methods for producing acetate compounds and alcohol compounds thereof, and compounds used for synthesizing the organic halogen compounds

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4057593A (en) * 1973-11-07 1977-11-08 Hoechst Aktiengesellschaft Process for preparing cis-olefins
US20130231499A1 (en) * 2012-03-05 2013-09-05 California Institute Of Technology Synthesis of z-olefin-containing lepidopteran insect pheromones
WO2014152309A1 (en) * 2013-03-14 2014-09-25 Materia, Inc. Use of soluble metal salts in metathesis reactions
US20170137365A1 (en) * 2015-11-18 2017-05-18 Provivi, Inc. Production of fatty olefin derivatives via olefin metathesis

Family Cites Families (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4231947A (en) 1979-01-02 1980-11-04 Massachusetts Institute Of Technology Tantalum and niobium catalysts or catalyst precursors
US4245131A (en) 1979-07-02 1981-01-13 Massachusetts Institute Of Technology Dimerization of olefins using tantalum and niobium catalysts
HU180386B (en) 1980-10-24 1983-02-28 Egyt Gyogyszervegyeszeti Gyar Process for producing 11-dodecen-1-ol and 11-dodecen-1-yl-acetate of insect-feromone activity
US4427595A (en) 1981-07-16 1984-01-24 Massachusetts Institute Of Technology Catalyst composition to effect metathesis of acetylenes
DE129474T1 (en) 1983-06-15 1985-08-29 Societe Nationale Elf Aquitaine, Courbevoie CATALYST FOR THE METATHESIS OF OLEFINS.
US4792620A (en) 1983-10-14 1988-12-20 Bp Chemicals Limited Carbonylation catalysts
US4727215A (en) 1985-09-25 1988-02-23 Massachusetts Institute Of Technology Catalyst composition for effecting metathesis of olefins
US4681956A (en) 1985-09-25 1987-07-21 Massachusetts Institute Of Technology Catalyst composition for effecting metathesis of olefins
US4837358A (en) 1986-02-26 1989-06-06 Phillips Petroleum Company Preparation of 9-alkenyl ester compounds
JPS62223136A (en) 1986-03-19 1987-10-01 Shin Etsu Chem Co Ltd 1-halo-(E,Z)-7,9-alkadiene compound
US5146033A (en) 1990-01-04 1992-09-08 Massachusetts Institute Of Technology Homogeneous rhenium catalysts for metathesis of olefins
US5087710A (en) 1990-01-04 1992-02-11 Massachusetts Institute Of Technology Homogeneous rhenium catalysts for metathesis of olefins
US5142073A (en) 1991-04-30 1992-08-25 Massachusetts Institute Of Technology Synthesis of molybdenum and tungsten complexes
EP0630877B1 (en) 1993-06-21 1997-03-12 Shin-Etsu Chemical Co., Ltd. Workup of Wittig reaction products
DE4434640C1 (en) 1994-09-28 1996-02-01 Hoechst Ag Bridged metallocene prodn. in-situ
DE19648637A1 (en) 1996-11-25 1998-06-04 Goldschmidt Ag Th Process for the preparation of alpha, omega-alkenols
US5916983A (en) 1997-05-27 1999-06-29 Bend Research, Inc. Biologically active compounds by catalytic olefin metathesis
SG72861A1 (en) 1997-09-30 2000-05-23 Kuraray Co Process for producing 7-octen-1-al
US6121473A (en) 1998-02-19 2000-09-19 Massachusetts Institute Of Technology Asymmetric ring-closing metathesis reactions
CN1208295C (en) 1998-04-01 2005-06-29 弗门尼舍有限公司 Reduction of carbonyl compounds by silanes in the presence of zinc catalysts
DE19815275B4 (en) 1998-04-06 2009-06-25 Evonik Degussa Gmbh Alkylidene complexes of ruthenium with N-heterocyclic carbene ligands and their use as highly active, selective catalysts for olefin metathesis
US6346652B1 (en) 1998-07-13 2002-02-12 Massachusetts Institute Of Technology Asymmetric ring-closing metathesis reactions involving achiral and meso substrates
WO2001036368A2 (en) * 1999-11-18 2001-05-25 Pederson Richard L Metathesis syntheses of pheromones or their components
US6215019B1 (en) * 1998-09-01 2001-04-10 Tilliechem, Inc. Synthesis of 5-decenyl acetate and other pheromone components
US6696597B2 (en) * 1998-09-01 2004-02-24 Tilliechem, Inc. Metathesis syntheses of pheromones or their components
EP1115491B1 (en) 1998-09-10 2009-08-05 University Of New Orleans Foundation Catalyst complex with phenylindenylidene ligand
JP3943015B2 (en) 2000-08-10 2007-07-11 トラスティーズ オブ ボストン カレッジ Recyclable metathesis catalyst
WO2002079126A1 (en) 2001-03-30 2002-10-10 California Institute Of Technology Cross-metathesis reaction of functionalized and substituted olefins using group 8 transition metal carbene complexes as metathesis catalysts
CA2473029A1 (en) 2002-01-22 2003-07-31 Universiteit Gent Ruthenium and osmium carbene complexes for use in metathesis
WO2004005223A1 (en) 2002-07-05 2004-01-15 Sasol Technology (Uk) Ltd Phosphorus containing ligands for metathesis catalysts
PL199412B1 (en) 2002-10-15 2008-09-30 Boehringer Ingelheim Int Ruthenium new complexes as (pre) catalytic agents of permutation reaction, new derivatives of 2-alkoxy-5-nitrostyrene as intermediate compounds and method of their receiving
EP1654060A4 (en) 2003-06-19 2007-08-08 Univ New Orleans Res & Technol Preparation of ruthenium-based olefin metathesis catalysts
EP1735352B1 (en) 2004-03-29 2019-08-21 California Institute Of Technology Latent, high-activity olefin metathesis catalysts containing an n-heterocyclic carbene ligand
JP5406525B2 (en) 2005-07-04 2014-02-05 ツァナン・サイテック・カンパニー・リミテッド Ruthenium complex ligand, ruthenium complex, immobilized ruthenium complex catalyst and preparation method and use thereof
GB0514612D0 (en) 2005-07-15 2005-08-24 Sasol Technology Uk Ltd The use of a phosphorus containing ligand and a cyclic organic ligand in a metathesis catalyst
EP1971616A1 (en) 2005-12-16 2008-09-24 Materia, Inc. Organometallic ruthenium complexes and related methods for the preparation of tetra-substituted and other hindered olefins
PL379879A1 (en) 2006-06-07 2007-12-10 Umicore Ag & Co.Kg. Ruthenium and osmium complex, the manner of their production and their application as (pre)catalytic agent of metathesis reaction
DE102006043704A1 (en) 2006-09-18 2008-03-27 Umicore Ag & Co. Kg New metathesis catalysts
DK2121546T3 (en) 2006-10-13 2018-03-12 Elevance Renewable Sciences Process for preparing omega-dicarboxylic acid olefin derivative by metathesis
US7932397B2 (en) 2006-11-22 2011-04-26 Massachusetts Institute Of Technology Olefin metathesis catalysts and related methods
FR2909382B1 (en) 2006-11-30 2009-01-23 Enscr RUTHENIUM CATALYTIC COMPLEXES AND THE USE OF SUCH COMPLEXES FOR OLEFIN METATHESIS
DE102007020694A1 (en) 2007-05-03 2008-11-06 Evonik Degussa Gmbh Sulfur-containing metathesis catalysts
FR2915995B1 (en) 2007-05-07 2012-05-25 Enscr CHIRAL LIGANDS OF N-HETEROCYCLIC CARBENE TYPE FOR ASYMMETRIC CATALYSIS.
JP5115368B2 (en) 2007-07-18 2013-01-09 三菱化学株式会社 Process for producing unsaturated alcohol
MX2010008110A (en) 2008-01-25 2011-03-04 Trustees Boston College Catalysts for metathesis reactons including enantioselective olefin metathesis, and related methods.
US8501975B2 (en) 2008-04-08 2013-08-06 Evonik Degussa Gmbh Method for manufacturing ruthenium carbene complexes
EP2276745A4 (en) 2008-04-09 2013-02-27 Materia Inc RUTHENIUM OLEFINE METATHESIS CATALYSTS HAVING SUBSTITUTED SKELETON N-HETEROCYCLIC CARBENE LIGANDS
JP5535217B2 (en) 2008-10-04 2014-07-02 ユミコア・アクチエンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト Method for producing ruthenium-indenylidenecarbene catalyst
US8222469B2 (en) 2009-07-15 2012-07-17 Massachusetts Institute Of Technology Catalysts and processes for the formation of terminal olefins by ethenolysis
US8362311B2 (en) 2009-09-30 2013-01-29 Massachusetts Institute Of Technology Highly Z-selective olefins metathesis
AP3604A (en) 2009-10-12 2016-02-25 Elevance Renewable Sciences Methods of refining and producing fuel from natural oil feedstocks
US9382502B2 (en) 2009-10-12 2016-07-05 Elevance Renewable Sciences, Inc. Methods of refining and producing isomerized fatty acid esters and fatty acids from natural oil feedstocks
PL2506972T3 (en) 2009-12-03 2019-09-30 Umicore Ag & Co. Kg Supported olefin metathesis catalysts
EP2361683A1 (en) 2010-01-29 2011-08-31 Umicore AG & Co. KG Process for preparation of ruthenium-based carbene catalysts with chelating alkylidene ligands
WO2011095991A2 (en) 2010-02-03 2011-08-11 Bhatt Manoj Kumar Natwarlal Composition for controlling mosquitos comprising an acyclic organosiloxane compound
EP2534140B1 (en) 2010-02-08 2018-04-11 Trustees of Boston College Efficient methods for z- or cis-selective cross-metathesis
US8546500B2 (en) 2011-05-27 2013-10-01 Massachusetts Institute Of Technology Complexes for use in metathesis reactions
CN103797009B (en) 2011-06-03 2017-04-26 麻省理工学院 Z-selective ring-closing metathesis reactions
PL216649B1 (en) 2011-06-06 2014-04-30 Univ Warszawski New ruthenium complexes, process for the preparation thereof and the use thereof in olefin metathesis reactions
US9085595B2 (en) 2011-11-07 2015-07-21 Massachusetts Institute Of Technology Tungsten oxo alkylidene complexes for Z selective olefin metathesis
PL230302B1 (en) 2012-02-27 2018-10-31 Apeiron Synthesis Spolka Z Ograniczona Odpowiedzialnoscia Metathesis catalysts containing onium groups
EP2639219B1 (en) 2012-03-14 2016-08-10 Umicore AG & Co. KG Ruthenium-based metathesis catalysts and precursors for their preparation
IN2014DN08906A (en) 2012-04-24 2015-05-22 Elevance Renewable Sciences
GB201208589D0 (en) 2012-05-16 2012-06-27 Givaudan Sa Improvements in or relating to organic compounds
PL2679593T3 (en) 2012-06-26 2018-08-31 Umicore Ag & Co. Kg Method for preparation of a ruthenium indenylidene complex
KR20150034679A (en) 2012-06-29 2015-04-03 아페이론 신세시스 에스.아. Metal complexes, their application and methods of carrying out a metathesis reaction
US8642814B1 (en) 2012-07-24 2014-02-04 Heliae Development, Llc Methods of converting mixtures of palmitoleic and oleic acid esters to high value products
PL400162A1 (en) 2012-07-27 2014-02-03 Apeiron Synthesis Spólka Z Ograniczona Odpowiedzialnoscia New ruthenium complexes, their use in metathesis reactions and the method of conducting metathesis reactions
CA2884257C (en) 2012-10-09 2022-07-26 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
EP2725030A1 (en) 2012-10-29 2014-04-30 Umicore AG & Co. KG Ruthenium-based metathesis catalysts, precursors for their preparation and their use
WO2014085393A1 (en) 2012-11-30 2014-06-05 Elevance Renewable Sciences Methods of making functionalized internal olefins and uses thereof
KR102211385B1 (en) 2013-02-27 2021-02-03 마터리아 인코포레이티드 Metal carbene olefin metathesis two catalyst composition
US9919299B2 (en) 2013-03-14 2018-03-20 Ximo Ag Metathesis catalysts and reactions using the catalysts
JP6431034B2 (en) 2013-03-14 2018-11-28 エレヴァンス リニューアブル サイエンシズ インコーポレイテッドElevance Renewable Sciences, Inc. Processed metathesis substrate material, its production and use
ES2910942T3 (en) 2013-03-15 2022-05-17 Dmitri Goussev Complex catalysts based on amino-phosphine ligands for hydrogenation and dehydrogenation processes
GB201305858D0 (en) 2013-03-28 2013-05-15 Ximo Ag Catalyst composition
US9315604B2 (en) 2013-04-09 2016-04-19 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
WO2014172534A1 (en) 2013-04-17 2014-10-23 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
US20140330018A1 (en) 2013-05-01 2014-11-06 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
PL3008078T3 (en) 2013-06-12 2019-06-28 Trustees Of Boston College Catalysts for efficient z-selective metathesis
US9441059B2 (en) 2013-06-20 2016-09-13 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
WO2015003815A1 (en) 2013-07-12 2015-01-15 Ximo Ag Immobilized metathesis tungsten catalysts and use thereof in olefin metathesis
CN103319704B (en) 2013-07-12 2015-06-17 南开大学 Method for preparing polyester through using 10-hendecenoic acid and vanillic acid
US10071950B2 (en) 2013-07-12 2018-09-11 Ximo Ag Use of immobilized molybdenum- and tungsten-containing catalysts in olefin cross metathesis
GB2522640B (en) 2014-01-30 2018-04-25 Univ Court Univ St Andrews Method of alkene metathesis
WO2015127192A1 (en) 2014-02-21 2015-08-27 Massachusetts Institute Of Technology Catalysts and methods for ring opening metathesis polymerization
GB201404468D0 (en) 2014-03-13 2014-04-30 Givaudan Sa Process
PL3129347T3 (en) 2014-04-10 2022-02-07 California Institute Of Technology Reactions in the presence of ruthenium complexes
GB201406591D0 (en) * 2014-04-11 2014-05-28 Ximo Ag Compounds
US9487471B1 (en) 2014-04-14 2016-11-08 Provivi, Inc. Synthesis of pyrethroids and pyrethroid-containing compositions
WO2016069308A1 (en) 2014-10-31 2016-05-06 Elevance Renewable Sciences, Inc. Terminally selective metathesis of polyenes derived from natural oil
MX2018015111A (en) 2016-06-06 2019-09-02 Provivi Inc Semi-biosynthetic production of fatty alcohols and fatty aldehydes.
CN110603240B (en) 2017-02-17 2022-11-15 普罗维维公司 Synthesis of pheromones and related substances by olefin metathesis

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4057593A (en) * 1973-11-07 1977-11-08 Hoechst Aktiengesellschaft Process for preparing cis-olefins
US20130231499A1 (en) * 2012-03-05 2013-09-05 California Institute Of Technology Synthesis of z-olefin-containing lepidopteran insect pheromones
WO2014152309A1 (en) * 2013-03-14 2014-09-25 Materia, Inc. Use of soluble metal salts in metathesis reactions
US20170137365A1 (en) * 2015-11-18 2017-05-18 Provivi, Inc. Production of fatty olefin derivatives via olefin metathesis

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